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Hello, everyone. Damian here with the fallout from Pfizer’s downbeat update, a new entrant in obesity research, and an orthogonal CRISPR business.

The need-to-know this morning

Apellis Pharmaceuticals said a European advisory committee is expected to recommend against the approval of Syfovre, its eye drug for a common form of blindness. The company plans to appeal the negative ruling.
Sage Therapeutics and Biogen announced the commercial launch of Zurzuvae, an oral treatment for women with postpartum depression.
Merck and Moderna reported three-year follow-up data on their mRNA-based immunotherapy for advanced melanoma. Phase 3 studies are underway.
The FDA accepted Amgen’s marketing application for tarlatamab, a bispecific antibody to treat advanced small cell lung cancer. The approval decision date is June 12, 2024.

Is it time to worry about Moderna?

Yesterday’s news that Pfizer is expecting to sell far fewer Covid-19 vaccines than Wall Street expected sent shares of Moderna down as much as 6% on fears that the company could be in for a painful revision of its own.

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Wikipedia

The need-to-know this morning

Is it time to worry about Moderna?

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United colonoscopy coverage change 'may cost lives,' doctors say

Illumina names Agilent executive as new CEO

Guidelines to prevent youth baseball injuries need more muscle

Snackable artificial intelligence, expert AI, and the pharma industry

Novavax promises a turnaround & Lilly roils the obesity market

How to fix cancer clinical trials' diversity problem

Bright Health sells Medicare Advantage business to Molina

Weighted lottery helped low

Hepatitis C has a cure — but many Americans still lack access to it

Medicaid rebukes states for mistakenly disenrolling children

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A strong 6.5

Vivek Ramaswamy, who's embraced Trump on the campaign trail, condemned him after Jan. 6

What American doctors can learn from their Israeli counterparts

Search resumes for 2 missing children washed away with mom in deadly Pennsylvania flash flood

Stem cell treatment guidelines are released by FDA

ER docs worry over extreme heat as a 'mass casualty event'

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